Canonical Allele Identifier: CA2021179084

Gene: GYS2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21563139A= , CM000674.2:g.21563139A=	GRCh38
NC_000012.11:g.21716073A= , CM000674.1:g.21716073A=	GRCh37
NC_000012.10:g.21607340A=	NCBI36
NG_016167.1:g.46709T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.941+89T= MANE Select	ENSP00000261195.2:n.941+89T=
ENST00000647960.1:c.*943+89T=	ENSP00000497202.1:n.*943+89T=
ENST00000648372.1:n.868+89T=
ENST00000261195.2:c.941+89T=	ENSP00000261195.2:n.941+89T=
NM_021957.3:c.941+89T=	NP_068776.2:n.941+89T=
XM_005253352.1:c.941+89T=	XP_005253409.1:n.941+89T=
XM_005253354.2:c.722+89T=	XP_005253411.1:n.722+89T=
XM_006719062.2:c.941+89T=	XP_006719125.1:n.941+89T=
XM_006719063.2:c.710+89T=	XP_006719126.1:n.710+89T=
NM_021957.4:c.941+89T= MANE Select	NP_068776.2:n.941+89T=
XM_006719063.3:c.710+89T=	XP_006719126.1:n.710+89T=
XM_017019245.2:c.941+89T=	XP_016874734.1:n.941+89T=
XM_024448960.1:c.941+89T=	XP_024304728.1:n.941+89T=